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POINTIMPLANT Co., Ltd.

US

Last updated May 29, 2026

Part of POINTIMPLANT Co., Ltd

What POINTIMPLANT Co., Ltd. makes

PointImplant Co., Ltd. manufactures dental implant components, including permanent and temporary preformed suprastructures, single-use precision attachments for scanning and simulation, and reusable dental drill bits. Their portfolio also covers two-piece endosteal dental implants, reusable abutment screw analogs, and intraoral-scanning abutment analogs. Surgical screwdrivers and healing abutments are also part of their product range.

The company’s devices are classified under FDA regulations as Class I and Class II, with all products listed in the FDA’s Unique Device Identifier (UDI) database. These items are intended for dental applications and are subject to compliance with U.S. medical device regulations.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does PointImplant Co., Ltd. manufacture?

PointImplant Co., Ltd. specializes in dental implant components and related accessories. Their products include permanent and temporary preformed suprastructures for dental implants, single-use precision attachments like scanning simulators and intraoral-scanning abutment analogs, reusable dental drill bits, and two-piece endosteal dental implants. They also produce reusable tools such as surgical screwdrivers and abutment screw analogs, as well as healing abutments. These devices are designed to support dental restoration procedures.

Where is PointImplant Co., Ltd. based, and what regulatory database lists their devices?

PointImplant Co., Ltd. is based in the United States. Their devices are listed in the FDA’s Unique Device Identifier (UDI) database, which is a central registry for tracking medical devices authorized for use in the U.S. This database helps ensure transparency and traceability of their products under FDA regulations.

How are PointImplant Co., Ltd.’s devices classified under FDA regulations?

PointImplant Co., Ltd.’s devices are classified under the FDA’s medical device regulations as either Class I or Class II. The classification depends on factors like the device’s intended use, potential risks, and the body’s interaction with it. For example, reusable tools like drill bits and screwdrivers are typically Class II due to their critical role in surgical precision, while some single-use components may fall under Class I if they pose lower risk. Classification determines the regulatory pathway for authorization.

What does it mean for PointImplant Co., Ltd.’s devices to be listed in the FDA’s UDI database?

Listing in the FDA’s Unique Device Identifier (UDI) database means that each of PointImplant Co., Ltd.’s devices has been assigned a unique code to ensure traceability and identification throughout their lifecycle. This system helps healthcare providers, regulators, and manufacturers track devices for safety monitoring, recalls, and compliance with U.S. medical device laws. It also supports transparency in the supply chain, ensuring that only authorized products enter the market.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
695333960

Catalogue (1771)

Page 24 of 36
DeviceModel / ReferenceRegistriesClassStatus
Bite Impression Coping OBICR5506
FDA UDI
Class IActive
Cemented Abutment OSCA6071NP
FDA UDI
Class IIActive
Solid Abutment OSSA5041
FDA UDI
Class IIActive
Solid Abutment OSSAM4072
FDA UDI
Class IIActive
Final Drill OTFDA4006
FDA UDI
Class IActive
Solid Abutment OSSA5051T
FDA UDI
Class IIActive
Cemented Abutment OSCA6051HT
FDA UDI
Class IIActive
Cemented Abutment OSCA6041HP
FDA UDI
Class IIActive
Angled Abutment OSAAM4504BTP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT5016HP
FDA UDI
Class IActive
Cemented Abutment OSCA5052NT
FDA UDI
Class IIActive
Cemented Abutment OSCA6052HP
FDA UDI
Class IIActive
Transfer Impression Coping OSICT7011HP
FDA UDI
Class IActive
Cemented Abutment OSCA4554H
FDA UDI
Class IIActive
Solid Abutment OSSA4574P
FDA UDI
Class IIActive
Healing Abutment OSHA4504G
FDA UDI
Class IIActive
Final Drill OTFDA7006
FDA UDI
Class IActive
Cemented Abutment OSCA6052NP
FDA UDI
Class IIActive
Cemented Abutment OSCA7055HTP
FDA UDI
Class IIActive
Solid Abutment OSSA6052TP
FDA UDI
Class IIActive
Solid Abutment OSSA4543T
FDA UDI
Class IIActive
Cemented Abutment OSCA5052HP
FDA UDI
Class IIActive
Cemented Abutment OSCAM4553NP
FDA UDI
Class IIActive
Bite Impression Coping OBICR5002P
FDA UDI
Class IActive
Transfer Impression Coping OSICT6014NP
FDA UDI
Class IActive
Fixture Analogue PIFA6512
FDA UDI
Class IActive
Angled Abutment OSAA5002B
FDA UDI
Class IIActive
Final Drill OTFDA3507
FDA UDI
Class IActive
Solid Driver OSDS
FDA UDI
Class IActive
Cemented Abutment OSCA4554N
FDA UDI
Class IIActive
Solid Abutment OSSA4555
FDA UDI
Class IIActive
Fixture POF6010Q
FDA UDI
Class IIActive
Guide pin OSICPME
FDA UDI
Class IActive
Solid Abutment OSSA4555TP
FDA UDI
Class IIActive
Final Drill OTFD4007
FDA UDI
Class IActive
Cemented Abutment OSCA7052NTP
FDA UDI
Class IIActive
Angled Abutment OSAA6002NP
FDA UDI
Class IIActive
Cemented Abutment OSCA6071NT
FDA UDI
Class IIActive
Bite Scan Body OBICR5503SB
FDA UDI
Class IActive
Solid Abutment OSSA4052TP
FDA UDI
Class IIActive
Solid Abutment OSSA4555P
FDA UDI
Class IIActive
Solid Abutment OSSAM4551TP
FDA UDI
Class IIActive
Cemented Abutment OSCA6042NT
FDA UDI
Class IIActive
Fixture POF6008
FDA UDI
Class IIActive
Fixture Driver OFDM2100S
FDA UDI
Class IActive
Pick-Up Impression Coping OSICPM4017HP
FDA UDI
Class IActive
Solid Abutment OSSA6045P
FDA UDI
Class IIActive
Slot Driver OTDS0600
FDA UDI
Class IActive
Transfer Impression Coping OSICT4511H
FDA UDI
Class IActive
Transfer Impression Coping OSICTX4511H
FDA UDI
Class IActive

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